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Synthesis, biological activity and molecular modeling of new biphenylic carboxamides as potent and selective CB2 receptor ligands

机译:作为有效和选择性CB2受体配体的新型联苯羧酰胺的合成,生物活性和分子建模

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摘要

The CB2 receptor is a therapeutic target of increasing importance for several diseases, including pain, inflammation, neurodegeneration, cancer and osteoporosis. While several compounds showing CB2-selective agonist or inverse agonist properties have been developed, only few CB2 receptor selective neutral antagonists are actually known. Such type of compounds could be useful to study more in depth the role of the CB2 receptor, because they lack the ability to counteract its "constitutive" activity. Here we describe the synthesis and biological activity of a series of biphenylic carboxamides as a new class of CB2 receptor selective ligands. In binding assays, one of these compounds showed good CB2 receptor affinity and selectivity (K-i = 11.48 nM; Selectivity Index = 130). Furthermore, in functional assays, the same compound showed a very interesting pharmacological profile as CB2 receptor selective neutral antagonist. These results pave the way to further developments, including structural optimization, with the aim to obtain more potent CB2 receptor ligands with this peculiar feature. (C) 2014 Elsevier Masson SAS. All rights reserved.
机译:CB2受体是对多种疾病(包括疼痛,炎症,神经退行性疾病,癌症和骨质疏松症)越来越重要的治疗目标。尽管已经开发出几种具有CB2选择性激动剂或反向激动剂特性的化合物,但实际上只有很少的CB2受体选择性中性拮抗剂是已知的。这种类型的化合物可用于更深入地研究CB2受体的作用,因为它们缺乏抵消其“组成”活性的能力。在这里,我们描述了一系列联苯羧酰胺作为一类新的CB2受体选择性配体的合成和生物活性。在结合测定中,这些化合物之一显示出良好的CB2受体亲和力和选择性(K-1 = 11.48 nM;选择性指数= 130)。此外,在功能测定中,相同的化合物显示出与CB2受体选择性中性拮抗剂非常相似的药理特性。这些结果为包括结构优化在内的进一步发展铺平了道路,目的是获得具有这种独特特征的更有效的CB2受体配体。 (C)2014 Elsevier Masson SAS。版权所有。

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